Kendall Curity Extension Tubes

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K892440 ↗

FDA Product Code

FPA

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Curity Venous Catheterization Kit

  Class II

  FDA 510(k) K861828 Active Cleared 10 Jul 1986

• Curity Fiberoptic Intubating Airway

  Class I

  FDA 510(k) K855137 Active Cleared 11 Mar 1986

• Curity Curad Bandages

  Class I

  FDA 510(k) K810126 Active Cleared 6 Feb 1981

• The Kendall Urinary Output Monitor

  Class I

  FDA 510(k) K852083 Active Cleared 20 Sep 1985

• Kendall Curity Irrigation Syringe

  Class II

  FDA 510(k) K892436 Active Cleared 14 Jul 1989

• Curity Continuous Epidural Anesthesia Tray

  Class II

  FDA 510(k) K871066 Active Cleared 15 May 1987

See all devices from The Kendal Co. →

• What are Kendall Curity Extension Tubes used for?

  Kendall Curity Extension Tubes are used as extension tubes in medical settings, providing a substantially equivalent solution.

• How are Kendall Curity Extension Tubes supplied?

  The Kendall Curity Extension Tubes are supplied by The Kendal Co., a reputable manufacturer in the medical device industry.

• What is the regulatory status of Kendall Curity Extension Tubes?

  Kendall Curity Extension Tubes have an FDA 510K authorization with the k number K892440, indicating substantial equivalence.